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Structure of 59236-38-3
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2-Amino-4-methyl-benzaldehyde features a strategically positioned amino group and methyl substituent that enhance electron density at the aromatic ring, enabling efficient coupling in Suzuki-Miyaura and Ullmann reactions. This bench-stable aldehyde integrates readily into heterocyclic scaffolds and serves as a key intermediate for bioactive molecule synthesis.
2-Amino-4-methylbenzaldehyde serves as a versatile building block in the synthesis of heterocyclic scaffolds and pharmaceutical intermediates. Its ortho-amino and aldehyde functionalities enable sequential transformations, including reductive amination, condensation reactions, and cyclization processes. The methyl group enhances electronic modulation and provides a handle for further functionalization. Bench-stable and readily purified by recrystallization, it functions effectively in multistep syntheses requiring precise regiocontrol and compatibility with common protecting groups.
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GHS Pictogram :
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GHS No : GHS07
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Signal Word : Warning
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UN#: N/A
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Class : N/A
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Packing Group : N/A
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Hazard Statements : H302
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Precautionary Statements : P264-P270-P330-P501
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Lot numbers can be found on the outside label of a product: